Chimeric nk receptor and methods for treating cancer

ABSTRACT

The present invention relates to chimeric immune receptor molecules for reducing or eliminating tumors. The chimeric receptors are composed a C-type lectin-like natural killer cell receptor, or a protein associated therewith, fused to an immune signaling receptor containing an immunoreceptor tyrosine-based activation motif. Methods for using the chimeric receptors are further provided.

This application claims the benefit of priority from U.S. provisionalpatent application Ser. Nos. 60/612,836, filed Sep. 24, 2004 and60/681,782, filed May 17, 2005, whose contents are incorporated hereinby reference in their entireties.

This invention was made in the course of research sponsored by theNational Cancer Institute (Grant No. CA 101748). The U.S. government mayhave certain rights in this invention.

BACKGROUND OF THE INVENTION

T cells, especially cytotoxic T cells, play important roles inanti-tumor immunity (Rossing and Brenner (2004) Mol. Ther. 10:5-18).Adoptive transfer of tumor-specific T cells into patients provides ameans to treat cancer (Sadelain, et al. (2003) Nat. Rev. Cancer3:35-45). However, the traditional approaches for obtaining largenumbers of tumor-specific T cells are time-consuming, laborious andsometimes difficult because the average frequency of antigen-specific Tcells in periphery is extremely low (Rosenberg (2001) Nature411:380-384; Ho, et al. (2003) Cancer Cell 3:431-437; Crowley, et al.(1990) Cancer Res. 50:492-498). In addition, isolation and expansion ofT cells that retain their antigen specificity and function can also be achallenging task (Sadelain, et al. (2003) supra). Genetic modificationof primary T cells with tumor-specific immunoreceptors, such asfull-length T cell receptors or chimeric T cell receptor molecules canbe used for redirecting T cells against tumor cells (Stevens, et al.(1995) J. Immunol. 154:762-771; Oelke, et al. (2003) Nat. Med.9:619-624; Stancovski, et al. (1993) J. Immunol. 151:6577-6582; Clay, etal. (1999) J. Immunol. 163:507-153). This strategy avoids the limitationof low frequency of antigen-specific T cells, allowing for facilitatedexpansion of tumor-specific T cells to therapeutic doses.

Natural killer (NK) cells are innate effector cells serving as a firstline of defense against certain viral infections and tumors (Biron, etal. (1999) Annu. Rev. Immunol. 17:189-220; Trinchieri (1989) Adv.Immunol. 47:187-376). They have also been implicated in the rejection ofallogeneic bone marrow transplants (Lanier (1995) Curr. Opin. Immunol.7:626-631; Yu, et al. (1992) Annu. Rev. Immunol. 10:189-214). Innateeffector cells recognize and eliminate their targets with fast kinetics,without prior sensitization. Therefore, NK cells need to sense if cellsare transformed, infected, or stressed to discriminate between abnormaland healthy tissues. According to the missing self phenomenon (Kärre, etal. (1986) Nature (London) 319:675-678), NK cells accomplish this bylooking for and eliminating cells with aberrant major histocompatibilitycomplex (MHC) class I expression; a concept validated by showing that NKcells are responsible for the rejection of the MHC class I-deficientlymphoma cell line RMA-S, but not its parental MHC class I-positive lineRMA.

Inhibitory receptors specific for MHC class I molecules have beenidentified in mice and humans. The human killer cell Ig-like receptors(KIR) recognize HLA-A, -B, or -C; the murine Ly49 receptors recognizeH-2K or H-2D; and the mouse and human CD94/NKG2 receptors are specificfor Qal^(b) or HLA-E, respectively (Long (1999) Annu. Rev. Immunol.17:875-904; Lanier (1998) Annu. Rev. Immunol. 16:359-393; Vance, et al.(1998) J. Exp. Med. 188:1841-1848).

Activating NK cell receptors specific for classic MHC class I molecules,nonclassic MHC class I molecules or MHC class I-related molecules havebeen described (Bakker, et al. (2000) Hum. Immunol. 61:18-27). One suchreceptor is NKG2D (natural killer cell group 2D) which is a C-typelectin-like receptor expressed on NK cells, γδ-TcR⁺ T cells, and CD8⁺αβ-TcR⁺ T cells (Bauer, et al. (1999) Science 285:727-730). NKG2D isassociated with the transmembrane adapter protein DAP10 (Wu, et al.(1999) Science 285:730-732), whose cytoplasmic domain binds to the p85subunit of the PI-3 kinase.

In humans, two families of ligands for NKG2D have been described (Bahram(2000)Adv. Immunol. 76:1-60; Cerwenka and Lanier (2001) Immunol. Rev.181:158-169). NKG2D binds to the polymorphic MHC class I chain-relatedmolecules (MIC)-A and MICE (Bauer, et al. (1999) supra). These areexpressed on many human tumor cell lines, on several freshly isolatedtumor specimens, and at low levels on gut epithelium (Groh, et al.(1999) Proc. Natl. Acad. Sci. USA 96:6879-6884). NKG2D also binds toanother family of ligands designated the UL binding proteins (ULBP)-1,-2, and -3 molecules (Cosman, et al. (2001) Immunity 14:123-133; Kubin,et al. (2001) Eur. J. Immunol. 31:1428-1437). Although similar to classI MHC molecules in their α1 and α2 domains, the genes encoding theseproteins are not localized within the MHC. Like MIC (Groh, et al. (1996)supra), the ULBP molecules do not associate with β₂-microglobulin orbind peptides. The known murine NKG2D-binding repertoire encompasses theretinoic acid early inducible-1 gene products (RAE-1) and the relatedH60 minor histocompatibility antigen (Cerwenka, et al. (2000) Immunity12:721-727; Diefenbach, et al. (2000) Nat. Immunol. 1:119-126). RAE-1and H60 were identified as ligands for mouse NKG2D by expression cloningthese cDNA from a mouse transformed lung cell line (Cerwenka, et al.(2000) supra). Transcripts of RAE-1 are rare in adult tissues butabundant in the embryo and on many mouse tumor cell lines, indicatingthat these are oncofetal antigens.

Recombinant receptors containing an intracellular domain for activatingT cells and an extracellular antigen-binding domain, which is typicallya single-chain fragment of a monoclonal antibody and is specific for atumor-specific antigen, are known in the art for targeting tumors fordestruction. See, e.g., U.S. Pat. No. 6,410,319.

Baba et al. ((2000) Hum. Immunol. 61:1202-18) teach KIR2□L1-CD3 zetachain chimeric proteins. Further, WO 02/068615 suggests fusion proteinsof NKG2D containing the external domain of NKG2D with a distinct DAP10interacting domain or with cytoplasmic domains derived from othersignaling molecules, for example CD28, for use in engineering cells thatrespond to NKG2D ligands and potentially create a system with enhancedsignaling capabilities.

U.S. Pat. No. 5,359,046 discloses a chimeric DNA sequence encoding amembrane bound protein, wherein the chimeric DNA comprises a DNAsequence encoding a signal sequence which directs the membrane boundprotein to the surface membrane; a DNA sequence encoding a non-MHCrestricted extracellular binding domain of a surface membrane proteinselected from the group consisting of CD4, CD8, IgG and single-chainantibody that binds specifically to at least one ligand, wherein saidligand is a protein on the surface of a cell or a viral protein; atransmembrane domain from a protein selected from the group consistingof CD4, CD8, IgG, single-chain antibody, the CD3 zeta chain, the CD3gamma chain, the CD3 delta chain and the CD3 epsilon chain; and acytoplasmic signal-transducing domain of a protein that activates anintracellular messenger system selected from the group consisting of theCD3 zeta chain, the CD3 gamma chain, the CD3 delta chain and the CD3epsilon chain, wherein the extracellular, domain and cytoplasmic domainare not naturally joined together and the cytoplasmic domain is notnaturally joined to an extracellular ligand-binding domain, and when thechimeric DNA is expressed as a membrane bound protein in a selected hostcell under conditions suitable for expression, the membrane boundprotein initiates signaling in the host cell.

SUMMARY OF THE INVENTION

The present invention is a nucleic acid construct for expressing achimeric receptor to reduce or eliminate a tumor. The nucleic acidconstruct contains a first nucleic acid sequence encoding a promoteroperably linked to a second nucleic acid sequence encoding a chimericreceptor protein comprising a C-type lectin-like natural killer cellreceptor, or a protein associated therewith, fused to an immunesignaling receptor having an immunoreceptor tyrosine-based activationmotif of SEQ ID NO:1. In one embodiment, the nucleic acid construct isin a vector. In particular embodiments, the nucleic acid constructfurther contains a suicide gene.

The present invention also relates to a method for reducing oreliminating tumors. The method involves introducing into an isolated Tcell of a patient having or suspected of having a tumor a nucleic acidconstruct containing a first nucleic acid sequence encoding a promoteroperably linked to a second nucleic acid sequence encoding a chimericreceptor protein comprising a C-type lectin-like natural killer cellreceptor, or a protein associated therewith, fused to an immunesignaling receptor having an immunoreceptor tyrosine-based activationmotif of SEQ ID NO:1. The T cell is subsequently injected back into thepatient so that the chimeric receptor is expressed on the surface of theT cell to activate anti-tumor immunity in the patent thereby reducing oreliminating the tumor.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates chimeric NK receptors exemplified herein.Extracellular (EC), transmembrane (TM), and cytoplasmic (Cyp) portionsare indicated. Wild-type (WT) and chimeric (CH) forms of the receptorsare indicated, wherein NH₂ denotes the N-terminus and COOH denotes theC-terminus.

FIG. 2 shows specific lysis of target cells by gene-modified primary Tcells. Effector T cells modified with vector only (shaded diamond),wild-type NKG2D (open square), murine chimeric NKG2D (shaded square),wild-type DAP10 (open triangle), murine chimeric DAP10 (shadedtriangle), or wild-type DAP12 (open circle) were co-cultured with targetcells RMA (Panel A), RMA/Rae-1β (Panel B), RMA/H60 (Panel C), YAC-1(Panel D), or EG7 (Panel E) cells, respectively, at ratios from 1:1 to25:1 in a 4 hour ⁵¹Cr release assay. The data are presented as mean±SDand representative of 3 to 5 independent experiments.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a chimeric receptor molecule composedof a natural killer cell receptor and an immune signaling receptorexpressed on the surface of a T cell to activate killing of a tumorcell. Nucleic acid sequences encoding the chimeric receptor molecule areintroduced into a patient's T-cells ex vivo and T-cells that express thechimeric receptor molecule are subsequently injected back into thepatient. In this manner, the chimeric receptor molecules provide a meansfor the patient's own immune cells to recognize and activate anti-tumorimmunity and establish long-term, specific, anti-tumor responses fortreating tumors or preventing regrowth of dormant or residual tumorcells. To prevent potential side effects that may occur fromuncontrolled inflammation or response against non-tumor tissue, suicidegenes are further introduced into the T-cells expressing the chimericreceptor molecule. The suicide gene is activated by administering anagent, specific for the suicide gene, to the patient thereby eliminatingall cells expressing the chimeric receptor molecule.

By way of illustration, murine chimeric receptor molecules composed ofNKG2D or Dap10 in combination with a N-terminally attached CD3ζ weregenerated and expressed in murine T-cells. NKG2D is a type II protein,in which the N-terminus is located intracellularly (Raulet (2003) Nat.Rev. Immunol. 3:781-790), whereas the CD3ζ chain is type I protein withthe C-terminus in the cytoplasm (Weissman, et al. (1988) Proc. Natl.Acad. Sci. USA 85:9709-9713). To generate a chimeric NKG2D-CD3ζ fusionprotein, an initiation codon ATG was placed ahead of the coding sequencefor the cytoplasmic region of the CD3ζ chain (without a stop codon TAA)followed by a wild-type NKG2D gene. Upon expression, the orientation ofthe CD3ζ portion is reversed inside the cells. The extracellular andtransmembrane domains are derived from NKG2D. A second chimeric geneencoding the Dap10 gene followed by a fragment coding for the CD3ζcytoplasmic domain was also constructed. The structures of the chimericand wild-type receptors used are diagrammed in FIG. 1.

To determine whether murine chimeric NKG2D or murine chimeric Dap10receptors could be expressed in a similar manner as wild-type murineNKG2D or Dap10, a NKG2D gene with an adaptor protein gene (Dap10/Dap12)were co-transfected into Bosc23 cells and NKG2D expression wasdetermined by flow cytometry. To analyze those cells that weretransfected, a bicistronic vector with a green fluorescent protein (GFP)gene controlled by an internal ribosome entry site (IRES) was used.NKG2D surface expression was normalized by gating on the GFP⁺ cellpopulation. Like many NK receptors, such as CD94/NKG2C, Ly49D, andLy49H, NKG2D needs to be associated with adaptor proteins (i.e., Dap10and/or Dap12) for surface expression (Raulet (2003) supra; Lanier (2003)Curr. Opin. Immunol. 15:308-314). Packaging cell Bosc23 did not expresseither NKG2D or Dap10/Dap12, and transfection with only one of the twocomponents did not give rise to surface expression of NKG2D. However,co-transfection of a NKG2D gene along with an adaptor protein gene ledto significant membrane expression of NKG2D. Compared with Dap12, Dap10transfection resulted in higher NKG2D surface expression. Surfaceexpression of NKG2D after association with chimeric Dap10 adaptor washigher than that with wild-type DAP10. Higher surface expression ofNKG2D was also observed after transfection with chimeric NKG2D than withwild-type NKG2D genes, especially when pairing with the Dap12 gene(>5-fold increase in MFI).

Concentrated, high-titer, retroviral vectors (ecotropic) were used toinfect C57BL/6 spleen cells, and NKG2D surface expression was determinedby flow cytometry seven days after retroviral transduction. Geneticmodification of T cells with wild-type Dap10, Dap12 and NKG2D did notsignificantly increase the surface expression of NKG2D (10-20%) comparedto vector alone. In contrast, significantly higher NKG2D expression wasobserved in T cells modified with either chimeric NKG2D (42%) orchimeric Dap10 (64%). In chimeric Dap10-transduced T cells, thesurface-expressed NKG2D molecules were only due to endogenous molecules,whereas both endogenous and exogenous NKG2D molecules were responsiblefor surface expression in chimeric NKG2D-modified T cells. Takentogether, these data indicate that chimeric NKG2D and chimeric Dap10molecules are expressed in a similar manner as the wild-type moleculesand that they increase NKG2D expression on T cells.

To assess whether the murine chimeric DAP10 or murine chimericNKG2D-transduced T cells were capable of recognizing NKG2D ligands,NKG2D ligand-positive tumor cells (RMA/Rae-1β, RMA/H60 and YAC-1) wereused as targets for chimeric NKG2D-bearing T cells. Chimeric DAP10 orchimeric NKG2D-transduced T cells produced high amounts of IFN-γ (20-30ng/mL) after co-culture with RMA/Rae-1β, RMA/H60 or YAC-1 cells(Table 1) but not with RMA cells (no ligands), indicating that thesechimeric NKG2D-modified T cells could functionally recognize NKG2Dligand-bearing tumor cells.

TABLE 1 IFN-γ (ng/mL ± SD) RMA/Rae- Construct Media RMA 1β RMA/H60 YAC-1Vector 0.03 ± 0.03 0.09 ± 0.18 0.02 ± 0.03 0.11 ± 0.63 0.84 ± 0.29 OnlyWild-type 0.01 ± 0.01 0.10 ± 0.21 0.04 ± 0.06 0.05 ± 0.00 1.08 ± 1.48NKG2D* Chimeric 0.07 ± 0.08 0.37 ± 0.34 4.70 ± 0.78 8.40 ± 1.60 17.80 ±4.60  NKG2D Wild-type 0.01 ± 0.10 0.11 ± 0.11 0.04 ± 0.03 0.09 ± 0.031.43 ± 1.72 DAP10* Chimeric 0.49 ± 0.55 0.82 ± 0.52 7.50 ± 4.40 18.60 ±7.60  28.70 ± 8.30  DAP10 Wild-Type 0.00 ± 0.01 0.00 ± 0.01 0.53 ± 0.670.13 ± 0.10 0.73 ± 0.09 DAP12^(#) *p = 0.74; ^(#)p = 0.56. Data arerepresentative of 3 experiments.

Similarly, chimeric human NKG2D-bearing CD8+ T cells secrete IFN-γ whenbrought into contact with human tumor cells from breast cancer (MCF-7,T47D), prostate cancer (DU145), pancreatic cancer (Pan-1), and melanomacancer (A375) (Table 2). T cells were cultured with irradiated tumorcells at a 4:1 ratio for 72 hours and IFN-γ was measured by ELISA. Tcells cultured without tumor cells functioned as a media only controlwhich produced no detectable IFN-γ. The specificity of the interactionwas evident by comparing chimeric NKG2D transduced T cells to vectoronly.

TABLE 2 IFN-γ (pg/mL ± SD) Construct T47D MCF-7 Panc-1 DU-145 A375Vector 28.9 53.5 97.2 61.4 262.4 Only (±12.5) (±3.6) (±8.0) (±4.2)(±44.2) Wild-type 35.2 43.6 115.8 84.4 200.5 NKG2D* (±30.0) (±9.2)(±89.8) (±47.1) (±79.5) Chimeric 130.3 2928.3 5028.1 4427.9 2609.2 NKG2D(±70.4) (±251.1) (±407.2) (±470.1) (±293.2) Tumor 23.4 17.7 26.6 27.411.4 Alone (±26.9) (±8.7) (±7.5) (±10.2) (±17.7)

In addition, upon NKG2D ligation, chimeric DAP10 or chimericNKG2D-modified T cells also released significant amounts ofproinflammatory chemokines (CCL3 and CCL5), as well as Th1 cytokines,GM-CSF and IL-3, but not Th2 cytokines IL-5 and IL-10. In contrast,wild-type Dap10, Dap12 or NKG2D alone-modified T cells did not show anysignificant response to the stimulation by RMA/Rae-1β, RMA/H60 or YAC-1cells. These data demonstrate that the chimeric molecules led to thedirect activation of T cells.

The cytotoxic activity of murine chimeric NKG2D-modified splenic T cellsagainst tumor cells was also determined. Chimeric Dap10 or chimericNKG2D-transduced T cells were able to lyse NKG2D ligand-expressingtarget cells (RMA/Rae-1β, RMA/H60, EG7 and YAC-1) in vitro (FIG. 2,Panels B-E). The specificity of the interaction was apparent from theabsence of lysis of YAC-1, EG7, RMA/Rae-13 and RMA/H60 cells by vectoronly-transduced T cells, and the lack of lysis of RMA cells by chimericDap10 or chimeric NKG2D-modified T cells (FIG. 2, Panel A). Similar tocytokine production, no significant specific lysis of tumor cells wasobserved by wild-type Dap10 or wild-type NKG2D-modified T cells. T cellstransduced with wild-type Dap12 were able to kill target cells thatexpressed ligands for NKG2D. Activated murine CD8+ T cells express NKG2D(associated with Dap10), so expression of Dap12 would allow theendogenous NKG2D to associate with Dap12 and provide a primaryactivation signal. It is noteworthy that T cells transduced with Dap12were three-to five-fold less efficient than T cells transduced withchimeric NK receptors at killing tumor cells. The killing of YAC-1 andEG7 tumor cells demonstrates that chimeric NK receptors provide the Tcells with a means to kill tumor cells that express endogenous NKG2Dligands.

These data demonstrated the need for NKG2D ligand expression on thetarget cells. To investigate the role of the NKG2D receptor, it wasdetermined whether blocking antibodies to NKG2D would diminish cytotoxicactivity. Chimeric NKG2D-transduced T cells killed RMA/Rae-1β and EG7tumor cells and this activity was reduced when anti-NKG2D antibodieswere included in the assay. Vector only-transduced T cells were unableto kill the target cells and the activity was not changed with theaddition of anti-NKG2D antibodies. While the data indicate that theNKG2D receptor was responsible for the activity in these assays, thechimeric receptors may have, in some way, altered the T cells to killvia their T cell receptor. To address this, the ability of chimericNKG2D-transduced T cells to kill RMA/Rae-1β tumor cells was examined.RMA-S cells are deficient in TAP genes and express very low levels ofMHC class I molecules on the cell surface and no MHC class II molecules(Aldrich, et al. (1992) J. Immunol. 149:3773-3777). ChimericNKG2D-bearing T cells killed RMA/Rae-1β tumor cells but not RMA-S cells.Vector-transduced T cells did not kill either RMA-S cell line. Thus,these data indicate that chimeric NKG2D functions via direct NKG2Drecognition of its ligand on target cells.

Having shown that chNKG2D-modified T cells could react against NKG2Dligand-positive tumor cells in vitro, the therapeutic potential ofchimeric NKG2D-modified T lymphocytes was determined in vivo. ChimericNKG2D-bearing T cells (10⁶) were co-injected with RMA/Rae-1β tumor cells(10⁵) subcutaneously to C57BL/6 mice. T cells transduced with thechimeric NKG2D construct significantly (P<0.05 at days 5-15) inhibitedthe growth of RMA/Rae-1β tumors compared with vector-transduced T cellsor tumor alone (Table 3). Approximately 36% ( 4/11) of chimericNKG2D-bearing T cell-treated mice were tumor-free after 30 days.Chimeric NKG2D-bearing T cells did not show any significant inhibitioneffects on the growth of wild-type RMA cells, indicating that inhibitionof RMA/Rae-1β tumor growth by chimeric NKG2D T cells was mediated bychimeric NKG2D-Rae-1β engagement.

TABLE 3 Tumor Area (Mean mm² ± SEM) T Cells transduced T cellstransduced with chimeric with vector only + Day NKG2D + RMA/Rae-1βRMA/Rae-1β RMA/Rae-1β 0 0.00 ± 0.00  0.00 ± 0.00 0.00 ± 0.00 5 0.00 ±0.00 16.14 ± 2.86 6.79 ± 1.47 7 3.10 ± 1.40 38.45 ± 3.79 28.69 ± 5.49  98.11 ± 3.09 57.40 ± 6.43 42.22 ± 6.38  11 11.84 ± 5.24   90.31 ± 11.6460.60 ± 12.10 13 14.73 ± 7.24  127.30 ± 16.85 82.67 ± 19.44 15 20.60 ±8.32  N.D. 110.51 ± 29.07  Results are a summary of three experiments.

In a second and more stringent model, transduced T cells (10⁷) wereadoptively transferred i.v. into B6 mice one day before s.c. tumorinoculation in the right flank. These chimeric NKG2D-bearing T cellssignificantly (P<0.05 at days 9-17) suppressed the growth of RMA/Rae-1βtumors (s.c.) compared with control vector-modified T cells (Table 4).As for the toxicity of treatment with chimeric NKG2D-modified T cells,the animals treated with chimeric NKG2D-bearing T cells did not show anyovert evidence of inflammatory damage (i.e., ruffled hair, hunchback ordiarrhea, etc.) indicating there was no overt toxicity.

TABLE 4 Tumor Area (Mean mm² ± SEM) T Cells transduced with Control Tcells with Day chimeric NKG2D Vector Only 5  3.06 ± 1.97 4.41 ± 2.20 712.14 ± 3.06 17.81 ± 1.75  9 13.94 ± 2.85 30.58 ± 3.87  11 25.92 ± 4.7745.13 ± 3.27  13 32.11 ± 5.84 64.83 ± 10.45 15 34.39 ± 9.77 80.72 ±13.34 17  37.81 ± 11.68 96.30 ± 14.15 Results are a summary of threeexperiments.

Because the immune system can select for tumor variants, the mosteffective immunotherapies for cancer are likely going to be those thatinduce immunity against multiple tumor antigens. Thus, it was testedwhether treatment with chimeric NKG2D-bearing T cells could induce hostimmunity against wild-type tumor cells. Mice that were treated withchimeric NKG2D-bearing T cells and RMA/Rae-1β tumor cells, and weretumor-free after 30 days, were challenged with RMA tumor cells. Thesetumor-free mice were resistant to a subsequent challenge of wild-typeRMA cells (10⁴), whereas all control naïve mice had aggressive tumors(tumor area: ˜100 mm²) after 2 weeks (Table 5). This observationindicates that adoptive transfer of chimeric NKG2D-bearing T cellsallows hosts to generate T cell memory.

TABLE 5 Tumor Area (Mean mm² ± SEM) Mice treated with T Cells transducedwith chimeric Day NKG2D + RMA/Rae-1β Näive Mice 5 0.00 ± 0.00  1.33 ±2.31 7 0.00 ± 0.00  11.65 ± 10.20 9 0.00 ± 0.00 38.75 ± 8.84 11 0.00 ±0.00 60.17 ± 6.10 13 0.00 ± 0.00 91.10 ± 5.59 15 0.00 ± 0.00 102.81 ±17.94 19 0.00 ± 0.00 146.71 ± 45.72 Results are a summary of threeexperiments.

In similar experiments, human chimeric receptor molecules composed ofNKG2D or Dap10 in combination with a N-terminally attached CD3ζ weregenerated and expressed in Bosc23 cells. Surface expression of NKG2D wasnot observed when either human Dap10 or human chimeric NKG2D weretransfected alone. However, co-transfection of a human chimeric NKG2D orhuman chimeric NKG2D-GFP gene along with a wild-type human DAP10 gene ormouse DAP10-GFP construct led to significant membrane expression ofNKG2D.

Binding of a human NKG2D fusion protein, composed of NKG2D with anN-terminally attached murine IgG1 Fc portion, to human NKG2D ligand onvarious tumor cell lines was assessed. Human NKG2D ligand was found tobe present on Jurkat (T lymphocyte origin), RPMI8866 (B cell origin),K562 (erythroid origin), Daubi (B cell origin), and U937 (monocyteorigin) tumor cell lines. Therefore, like the mouse chimeras, a humanchimeric NKG2D construct can functionally recognize NKG2D ligand-bearingtumor cells.

The cytotoxic activity of human chimeric NKG2D-modified T cells againsttumor cells was also determined. Human chimeric NKG2D-transduced primaryhuman T cells were able to lyse mastocytoma cell line P815 transducedwith human MIC-A (P815/MICA-A) in vitro (Table 6). The specificity ofthe interaction was apparent from the absence of lysis of wild-type P815tumor cells and the absence of lysis by vector only-transduced T cells.

TABLE 6 Specific Lysis (%) Tumor Cell Line Effector:Target P815/MIC-AP815 Ratio 1 5 25 1 5 25 Vector Only 0.0 0.0 0.6 0.0 −0.6 0.0 Humanchimeric 5.4 17.3 35.4 −2.5 −0.3 1.1 NKG2D

Further, blocking of human chimeric NKG2D with an anti-NKG2D antibodyprevented killing of K562 and RPMI8866 tumor cells by chimericNKG2D-transduced human T cells (Table 7). These data demonstratereceptor specificity because a control antibody could not preventkilling.

TABLE 7 Specific Lysis (%) Tumor Cell Line Effector:Target K562 RPMI8866Ratio 1 5 25 1 5 25 Vector + control 0.0 0.3 2.3 0.0 1.0 0.0 antibodyVector + anti- 0.0 0.7 2.1 0.0 1.0 1.3 NKG2D antibody Human chimeric 3.117.6 53.8 9.3 27.4 41.6 NKG2D + control antibody Human chimeric 1.6 10.127.0 1.0 2.5 7.5 NKG2D + anti- NKG2D antibody

Similar to the mouse studies, human chimeric NKG2D-transduced T cellsproduced high amounts of IFN-γ (˜150-2250 pg/mL) after a 24 hourco-culture with tumor cells that express ligands for NKG2D (i.e.,Jurkat, RPMI8866, K652, ECC-01 and P815/MIC-A tumor cells) compared withtumor cells that do not express NKG2D ligands (P815) or T cellsincubated alone (Table 8). Vector only-transduced T cells did notproduce IFN-γ, except against RPMI8866, indicating another ligand onthis cell type for these activated T cells; however, IFN-γ productionwas almost 10-times as high with the human chimeric NKG2D-bearing Tcells. Tumor cells alone produce no detectable IFN-γ.

TABLE 8 IFN-γ (Mean pg/mL ± SD) Tumor cell Tumor cell Type ChimericNKG2D Vector Only control P815 30.32 ± 1.31 15.11 ± 0.94  5.53 ± 1.31P815/MIC-A 140.19 ± 5.91  9.19 ± 3.30 2.85 ± 1.50 Jurkat 182.66 ± 18.317.64 ± 1.04 2.83 ± 1.33 RPMI8866 2239.95 ± 19.59  280.41 ± 13.84  2.47 ±2.47 K652 2305.46 ± 75.84  1.91 ± 0.57 1.82 ± 1.39 ECC-1 469.97 ± 18.792.67 ± 2.67 0.00 ± 0.00 T Cells only 13.67 ± 2.55 0.94 ± 0.54 N.D.Amounts represent the average of three experiments

Thus, having demonstrated the activation of host anti-tumor immunity andtumor elimination using chimeric NK cell receptors expressed in the Tcells of an animal model of cancer and likewise demonstrated human tumorcell killing with human chimeric NK cell receptors, the presentinvention relates to a nucleic acid construct for expressing a chimericreceptor in host T cells to reduce or eliminate a tumor. The nucleicacid construct contains a first nucleic acid sequence encoding apromoter operably linked to a second nucleic acid sequence encoding achimeric receptor protein containing a C-type lectin-like natural killercell receptor, or a protein associated therewith, fused to an immunesignaling receptor having an immunoreceptor tyrosine-based activationmotif of SEQ ID NO:1. In general, the C-type lectin-like NK cell type IIreceptor (or a protein associated therewith) is located at theC-terminus of the chimeric receptor protein of the present inventionwhereas the immune signaling receptor is at the N-terminus, therebyfacilitating intracellular signal transduction from the C-typelectin-like NK cell type II receptor.

A C-type lectin-like NK cell receptor protein particularly suitable foruse in the chimeric receptor of the present invention includes areceptor expressed on the surface of natural killer cells, wherein uponbinding to its cognate ligand(s) it alters NK cell activation. Thereceptor can work alone or in concert with other molecules. Ligands forthese receptors are generally expressed on the surface of one or moretumor cell types, e.g., tumors associated with cancers of the colon,lung, breast, kidney, ovary, cervix, and prostate; melanomas; myelomas;leukemias; and lymphomas (Wu, et al. (2004) J. Clin. Invest. 114:60-568;Groh, et al. (1999) Proc. Natl. Acad. Sci. USA 96:6879-6884; Pende, etal. (2001) Eur. J. Immunol. 31:1076-1086) and are not widely expressedon the surface of cells of normal tissues. Examples of such ligandsinclude, but are not limited to, MIC-A, MIC-B, heat shock proteins, ULBPbinding proteins (e.g., ULPBs 1-4), and non-classical HLA molecules suchas HLA-E and HLA-G, whereas classical MHC molecules such as HLA-A,HLA-B, or HLA-C and alleles thereof are not generally considered strongligands of the C-type lectin-like NK cell receptor protein of thepresent invention. C-type lectin-like NK cell receptors which bind theseligands generally have a type II protein structure, wherein theN-terminal end of the protein is intracellular. Exemplary NK cellreceptors of this type include, but are not limited to, Dectin-1(GENBANK accession number AJ312373 or AJ312372), Mast cellfunction-associated antigen (GENBANK accession number AF097358),HNKR-P1A (GENBANK accession number U11276), LLT1 (GENBANK accessionnumber AF133299), CD69 (GENBANK accession number NM_(—)001781), CD69homolog, CD72 (GENBANK accession number NM_(—)001782), CD94 (GENBANKaccession number NM_(—)002262 or NM_(—)007334), KLRF1 (GENBANK accessionnumber NM_(—)016523), Oxidised LDL receptor (GENBANK accession numberNM_(—)002543), CLEC-1, CLEC-2 (GENBANK accession number NM_(—)016509),NKG2D (GENBANK accession number BCO39836), NKG2C (GENBANK accessionnumber AJ001684), NKG2A (GENBANK accession number AF461812), NKG2E(GENBANK accession number AF461157), WUGSC:H_DJ0701016.2, or MyeloidDAP12-associating lectin (MDL-1; GENBANK accession number AJ271684). Inparticular embodiments, the NK cell receptor is human NKG2D (SEQ IDNO:2) or human NKG2C (SEQ ID NO:3).

Similar type I receptors which would be useful in the chimeric receptorof the present invention include NKp46 (e.g., GENBANK accession numberAJ001383), NKp30 (e.g., GENBANK accession number AB055881), or NKp44(e.g., GENBANK accession number AJ225109).

As an alternative to the C-type lectin-like NK cell receptor protein, aprotein associated with a C-type lectin-like NK cell receptor proteincan be used in the chimeric receptor protein of the present invention.In general, proteins associated with C-type lectin-like NK cell receptorare defined as proteins that interact with the receptor and transducesignals therefrom. Suitable human proteins which function in this mannerinclude, but are not limited to DAP10 (e.g., GENBANK accession numberAF072845; SEQ ID NO:4) and DAP12 (e.g., GENBANK accession numberAF019562; SEQ ID NO:5).

To the N-terminus of the C-type lectin-like NK cell receptor is fused animmune signaling receptor having an immunoreceptor tyrosine-basedactivation motif (ITAM),(Asp/Glu)-Xaa-Xaa-Tyr*-Xaa-Xaa-(Ile/Leu)-Xaa₆₋₈-Tyr*-Xaa-Xaa-(Ile/Leu)(SEQ ID NO:1) which is involved in the activation of cellular responsesvia immune receptors. Similarly, when employing a protein associatedwith a C-type lectin-like NK cell receptor, an immune signaling receptorcan be fused to the C-terminus of said protein (FIG. 1). Suitable immunesignaling receptors for use in the chimeric receptor of the presentinvention include, but are not limited to, the zeta chain of the T-cellreceptor, the eta chain which differs from the zeta chain only in itsmost C-terminal exon as a result of alternative splicing of the zetamRNA, the delta, gamma and epsilon chains of the T-cell receptor (CD3chains) and the gamma subunit of the FcR1 receptor. In particularembodiments, the immune signaling receptor is CD3-zeta (CD3) (e.g.,GENBANK accession number human NM_(—)198053; SEQ ID NO:6), or human Fcepsilon receptor-gamma chain (e.g., GENBANK accession number M33195; SEQID NO:7) or the cytoplasmic domain or a splicing variant thereof.

In particular embodiments, a chimeric receptor of the present inventionis a fusion between NKG2D and CD3ζ or Dap10 and CD3ζ.

As used herein, a nucleic acid construct or nucleic acid sequence isintended to mean a DNA molecule which can be transformed or introducedinto a T cell and be transcribed and translated to produce a product(e.g., a chimeric receptor or a suicide protein).

In the nucleic acid construct of the present invention, the promoter isoperably linked to the nucleic acid sequence encoding the chimericreceptor of the present invention, i.e., they are positioned so as topromote transcription of the messenger RNA from the DNA encoding thechimeric receptor. The promoter can be of genomic origin orsynthetically generated. A variety of promoters for use in T cells arewell-known in the art (e.g., the CD4 promoter disclosed by Marodon, etal. (2003) Blood 101(9):3416-23). The promoter can be constitutive orinducible, where induction is associated with the specific cell type ora specific level of maturation. Alternatively, a number of well-knownviral promoters are also suitable. Promoters of interest include theβ-actin promoter, SV40 early and late promoters, immunoglobulinpromoter, human cytomegalovirus promoter, retrovirus promoter, and theFriend spleen focus-forming virus promoter. The promoters may or may notbe associated with enhancers, wherein the enhancers may be naturallyassociated with the particular promoter or associated with a differentpromoter.

The sequence of the open reading frame encoding the chimeric receptorcan be obtained from a genomic DNA source, a cDNA source, or can besynthesized (e.g., via PCR), or combinations thereof. Depending upon thesize of the genomic DNA and the number of introns, it may be desirableto use cDNA or a combination thereof as it is found that intronsstabilize the mRNA or provide T cell-specific expression (Barthel andGoldfeld (2003) J. Immunol. 171(7):3612-9). Also, it may be furtheradvantageous to use endogenous or exogenous non-coding regions tostabilize the mRNA.

For expression of a chimeric receptor of the present invention, thenaturally occurring or endogenous transcriptional initiation region ofthe nucleic acid sequence encoding N-terminal component of the chimericreceptor can be used to generate the chimeric receptor in the targethost. Alternatively, an exogenous transcriptional initiation region canbe used which allows for constitutive or inducible expression, whereinexpression can be controlled depending upon the target host, the levelof expression desired, the nature of the target host, and the like.

Likewise, the signal sequence directing the chimeric receptor to thesurface membrane can be the endogenous signal sequence of N-terminalcomponent of the chimeric receptor. Optionally, in some instances, itmay be desirable to exchange this sequence for a different signalsequence. However, the signal sequence selected should be compatiblewith the secretory pathway of T cells so that the chimeric receptor ispresented on the surface of the T cell.

Similarly, a termination region can be provided by the naturallyoccurring or endogenous transcriptional termination region of thenucleic acid sequence encoding the C-terminal component of the chimericreceptor. Alternatively, the termination region can be derived from adifferent source. For the most part, the source of the terminationregion is generally not considered to be critical to the expression of arecombinant protein and a wide variety of termination regions can beemployed without adversely affecting expression.

As will be appreciated by one of skill in the art, in some instances, afew amino acids at the ends of the C-type lectin-like natural killercell receptor (or protein associated therewith) or immune signalingreceptor can be deleted, usually not more than 10, more usually not morethan 5 residues. Also, it may be desirable to introduce a small numberof amino acids at the borders, usually not more than 10, more usuallynot more than 5 residues. The deletion or insertion of amino acids willusually be as a result of the needs of the construction, providing forconvenient restriction sites, ease of manipulation, improvement inlevels of expression, or the like. In addition, the substitute of one ormore amino acids with a different amino acid can occur for similarreasons, usually not substituting more than about five amino acids inany one domain.

The chimeric construct, which encodes the chimeric receptor according tothis invention can be prepared in conventional ways. Since, for the mostpart, natural sequences are employed, the natural genes are isolated andmanipulated, as appropriate (e.g., when employing a Type II receptor,the immune signaling receptor component may have to be inverted), so asto allow for the proper joining of the various components. Thus, thenucleic acid sequences encoding for the N-terminal and C-terminalproteins of the chimeric receptor can be isolated by employing thepolymerase chain reaction (PCR), using appropriate primers which resultin deletion of the undesired portions of the gene. Alternatively,restriction digests of cloned genes can be used to generate the chimericconstruct. In either case, the sequences can be selected to provide forrestriction sites which are blunt-ended, or have complementary overlaps.

The various manipulations for preparing the chimeric construct can becarried out in vitro and in particular embodiments the chimericconstruct is introduced into vectors for cloning and expression in anappropriate host using standard transformation or transfection methods.Thus, after each manipulation, the resulting construct from joining ofthe DNA sequences is cloned, the vector isolated, and the sequencescreened to insure that the sequence encodes the desired chimericreceptor. The sequence can be screened by restriction analysis,sequencing, or the like.

The chimeric constructs of the present invention find application insubjects having or suspected of having cancer by reducing the size of atumor or preventing the growth or regrowth of a tumor in these subjects.Accordingly, the present invention further relates to a method forreducing growth or preventing tumor formation in a subject byintroducing a chimeric construct of the present invention into anisolated T cell of the subject and reintroducing into the subject thetransformed T cell thereby effecting anti-tumor responses to reduce oreliminate tumors in the subject. Suitable T cells which can be usedinclude, cytotoxic lymphocytes (CTL), tumor-infiltrating-lymphocytes(TIL) or other cells which are capable of killing target cells whenactivated. As is well-known to one of skill in the art, various methodsare readily available for isolating these cells from a subject. Forexample, using cell surface marker expression or using commerciallyavailable kits (e.g., ISOCELL™ from Pierce, Rockford, Ill.).

While the present invention relates to the elimination of tumors, thechimeric NK receptors of the present invention may also be useful fortreatment of other diseases where these ligands may be present. Forexample, the immune response can be down-modulated during autoimmunedisease or transplantation by expressing these type of chimeric NKreceptors in T regulatory or T suppressor cells. Thus, these cells wouldmediate their regulatory/suppressive function only in the location wherethe body has upregulated one of the ligands for these receptors. Thisligand upregulation may occur during stress or inflammatory responses.

It is contemplated that the chimeric construct can be introduced intothe subject's own T cells as naked DNA or in a suitable vector. Methodsof stably transfecting T cells by electroporation using naked DNA areknown in the art. See, e.g., U.S. Pat. No. 6,410,319. Naked DNAgenerally refers to the DNA encoding a chimeric receptor of the presentinvention contained in a plasmid expression vector in proper orientationfor expression. Advantageously, the use of naked DNA reduces the timerequired to produce T cells expressing the chimeric receptor of thepresent invention.

Alternatively, a viral vector (e.g., a retroviral vector, adenoviralvector, adeno-associated viral vector, or lentiviral vector) can be usedto introduce the chimeric construct into T cells. Suitable vectors foruse in accordance with the method of the present invention arenon-replicating in the subject's T cells. A large number of vectors areknown which are based on viruses, where the copy number of the virusmaintained in the cell is low enough to maintain the viability of thecell. Illustrative vectors include the pFB-neo vectors (STRATAGENE®)disclosed herein as well as vectors based on HIV, SV40, EBV, HSV or BPV.

Once it is established that the transfected or transduced T cell iscapable of expressing the chimeric receptor as a surface membraneprotein with the desired regulation and at a desired level, it can bedetermined whether the chimeric receptor is functional in the host cellto provide for the desired signal induction (e.g., production of Rantes,Mipl-alpha, GM-CSF upon stimulation with the appropriate ligand).

Subsequently, the transduced T cells are reintroduced or administered tothe subject to activate anti-tumor responses in said subject. Tofacilitate administration, the transduced T cells according to theinvention can be made into a pharmaceutical composition or made implantappropriate for administration in vivo, with appropriate carriers ordiluents, which further can be pharmaceutically acceptable. The means ofmaking such a composition or an implant have been described in the art(see, for instance, Remington's Pharmaceutical Sciences, 16th Ed., Mack,ed. (1980)). Where appropriate, the transduced T cells can be formulatedinto a preparation in semisolid or liquid form, such as a capsule,solution, injection, inhalant, or aerosol, in the usual ways for theirrespective route of administration. Means known in the art can beutilized to prevent or minimize release and absorption of thecomposition until it reaches the target tissue or organ, or to ensuretimed-release of the composition. Desirably, however, a pharmaceuticallyacceptable form is employed which does not ineffectuate the cellsexpressing the chimeric receptor. Thus, desirably the transduced T cellscan be made into a pharmaceutical composition containing a balanced saltsolution, preferably Hanks' balanced salt solution, or normal saline.

A pharmaceutical composition of the present invention can be used aloneor in combination with other well-established agents useful for treatingcancer. Whether delivered alone or in combination with other agents, thepharmaceutical composition of the present invention can be delivered viavarious routes and to various sites in a mammalian, particularly human,body to achieve a particular effect. One skilled in the art willrecognize that, although more than one route can be used foradministration, a particular route can provide a more immediate and moreeffective reaction than another route. For example, intradermal deliverymay be advantageously used over inhalation for the treatment ofmelanoma. Local or systemic delivery can be accomplished byadministration comprising application or instillation of the formulationinto body cavities, inhalation or insufflation of an aerosol, or byparenteral introduction, comprising intramuscular, intravenous,intraportal, intrahepatic, peritoneal, subcutaneous, or intradermaladministration.

A composition of the present invention can be provided in unit dosageform wherein each dosage unit, e.g., an injection, contains apredetermined amount of the composition, alone or in appropriatecombination with other active agents. The term unit dosage form as usedherein refers to physically discrete units suitable as unitary dosagesfor human and animal subjects, each unit containing a predeterminedquantity of the composition of the present invention, alone or incombination with other active agents, calculated in an amount sufficientto produce the desired effect, in association with a pharmaceuticallyacceptable diluent, carrier, or vehicle, where appropriate. Thespecifications for the novel unit dosage forms of the present inventiondepend on the particular pharmacodynamics associated with thepharmaceutical composition in the particular subject.

Desirably an effective amount or sufficient number of the isolatedtransduced T cells is present in the composition and introduced into thesubject such that long-term, specific, anti-tumor responses areestablished to reduce the size of a tumor or eliminate tumor growth orregrowth than would otherwise result in the absence of such treatment.Desirably, the amount of transduced T cells reintroduced into thesubject causes a 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%,or 100% decrease in tumor size when compared to otherwise sameconditions wherein the transduced T cells are not present.

Accordingly, the amount of transduced T cells administered should takeinto account the route of administration and should be such that asufficient number of the transduced T cells will be introduced so as toachieve the desired therapeutic response. Furthermore, the amounts ofeach active agent included in the compositions described herein (e.g.,the amount per each cell to be contacted or the amount per certain bodyweight) can vary in different applications. In general, theconcentration of transduced T cells desirably should be sufficient toprovide in the subject being treated at least from about 1×10⁸ to about1×10⁹ transduced T cells, even more desirably, from about 1×10⁷ to about5×10⁸ transduced T cells, although any suitable amount can be utilizedeither above, e.g., greater than 5×10⁸ cells, or below, e.g., less than1×10⁷ cells. The dosing schedule can be based on well-establishedcell-based therapies (see, e.g., Topalian and Rosenberg (1987) ActaHaematol. 78 Suppl 1:75-6; U.S. Pat. No. 4,690,915) or an alternatecontinuous infusion strategy can be employed.

These values provide general guidance of the range of transduced T cellsto be utilized by the practitioner upon optimizing the method of thepresent invention for practice of the invention. The recitation hereinof such ranges by no means precludes the use of a higher or lower amountof a component, as might be warranted in a particular application. Forexample, the actual dose and schedule can vary depending on whether thecompositions are administered in combination with other pharmaceuticalcompositions, or depending on interindividual differences inpharmacokinetics, drug disposition, and metabolism. One skilled in theart readily can make any necessary adjustments in accordance with theexigencies of the particular situation.

In particular embodiments, the chimeric nucleic acid construct furthercontains a suicide gene such as thymidine kinase (TK) of the HSV virus(herpesvirus) type I (Bonini, et al. (1997) Science 276:1719-1724), aFas-based “artificial suicide gene” (Thomis, et al. (2001) Blood97:1249-1257), or E. coli cytosine deaminase gene which are activated bygancyclovir, AP1903, or 5-fluorocytosine, respectively. The suicide geneis advantageously included in the nucleic acid construct of the presentinvention to provide for the opportunity to ablate the transduced Tcells in case of toxicity and to destroy the chimeric construct once atumor has been reduced or eliminated. The use of suicide genes foreliminating transformed or transduced cells is well-known in the art.For example, Bonini, et al. ((1997) Science 276:1719-1724) teach thatdonor lymphocytes transduced with the HSV-TK suicide gene provideantitumor activity in patients for up to one year and elimination of thetransduced cells is achieved using ganciclovir. Further, Gonzalez, etal. ((2004) J. Gene Med. 6:704-711) describe the targeting ofneuroblastoma with cytotoxic T lymphocyte clones genetically modified toexpress a chimeric scFvFc: ζ immunoreceptor specific for an epitope onL1-CAM, wherein the construct further expresses the hygromycin thymidinekinase (HyTK) suicide gene to eliminate the transgenic clones.

It is contemplated that the suicide gene can be expressed from the samepromoter as the chimeric receptor or from a different promoter.Generally, however, nucleic acid sequences encoding the suicide proteinand chimeric receptor reside on the same construct or vector. Expressionof the suicide gene from the same promoter as the chimeric receptor canbe accomplished using any well-known internal ribosome entry site(IRES). Suitable IRES sequences which can be used in the nucleic acidconstruct of the present invention include, but are not limited to, IRESfrom EMCV, c-myc, FGF-2, poliovirus and HTLV-1. By way of illustration,a nucleic acid construct for expressing a chimeric receptor can have thefollowing structure: promoter->chimeric receptor->IRES->suicidal gene.Alternatively, the suicide gene can be expressed from a differentpromoter than that of the chimeric receptor (e.g., promoter 1->chimericreceptor->promoter 2->suicidal gene).

The following non-limiting examples are presented to better illustratethe invention.

Example 1 Mice and Cell Lines

C57BL/6 mice were purchased from the National Cancer Institute, and allanimal work was conducted in accordance with standard guidelines.

Cell lines Bosc23, PT67, GP+E86, EG7 (H-2^(b)), and YAC-1 were obtainedfrom the American Type Culture Collection (ATCC, Rockville, Md.). RMAcells (H-2^(b)) originated from a Rauscher virus-induced C57BL/6 T-celllymphoma (Ljunggren and Karre (1985) J. Exp. Med. 162:1745-1759). RMAS-Sis a sub-line of RMA which lacks MHC class-I surface expression (Kärre,et al. (1986) Nature 319:675-678). All packaging cells were grown inDulbecco's modified Eagle medium (DMEM) with a high glucoseconcentration (4.5 gram/liter) supplemented with 10% heat-inactivatedfetal bovine serum (FBS; Hyclone, Logan, Utah), 20 U/mL penicillin, 20μg/mL streptomycin, 1 mM pyruvate, 10 mM HEPES, 0.1 mM non-essentialamino acids, 50 μM 2-mercaptoethanol. RMA, EG7, RMA-S and YAC-1 cellswere cultured in RPMI plus the same supplements described above.

Example 2 Retroviral Vector Construction

The full-length murine NKG2D cDNA was purchased from Open Biosystems(Huntsville, Ala.). Murine CD3ζ chain, Dap10 and Dap12 cDNAs were clonedby RT-PCR using RNAs from ConA- or IL-2 (1000 U/mL)-activated spleencells as templates. Mouse NKG2D ligands Rae-1β and H60 were cloned fromYAC-1 cells by RT-PCR. All PCR reactions were performed usinghigh-fidelity enzyme Pfu or PFUULTRA™ (STRATAGENE®, La Jolla, Calif.).The oligonucleotides employed in these PCR reactions are listed in Table9.

TABLE 9 SEQ ID No. Primer Sequence NO: 1 5′ wtNKG2DGCGAATTCGCCACCATGGCATT 8 GATTCGTGATCGA 2 3′ wtNKG2DGGCGCTCGAGTTACACCGCCCT 9 TTTCATGCAGAT 3 5′ chNKG2DGGCGAATTCGCATTGATTCGTG 10 ATCGAAAGTCT 4 5′ wtDAP10GCAAGTCGACGCCACCATGGAC 11 CCCCCAGGCTACC 5 3′ wtDAP10GGCGAATTCTCAGCCTCTGCCA 12 GGCATGTTGAT 6 3′ chDAP10GGCAGAATTCGCCTCTGCCAGG 13 CATGTTGATGTA 7 5′ wtDAP12GTTAGAATTCGCCACCATGGGG 14 GCTCTGGAGCCCT 8 3′ wtDAP12GCAACTCGAGTCATCTGTAATA 15 TTGCCTCTGTG 9 5′ ATG-CD3ζGGCGTCGACACCATGAGAGCAA 16 AATTCAGCAGGAG 10 3′ ATG-CD3ζGCTTGAATTCGCGAGGGGCCAG 17 GGTCTGCATAT 11 5′ CD3ζ-TAAGCAGAATTCAGAGCAAAATTCA 18 GCAGGAGTGC 12 3′ CD3ζ-TAAGCTTTCTCGAGTTAGCGAGGGG 19 CCAGGGTCTGCAT 13 5′ Rae-1GCATGTCGACGCCACCATGGCC 20 AAGGCAGCAGTGA 14 3′ Rae-1GCGGCTCGAGTCACATCGCAAA 21 TGCAAATGC 15 5′ H60 GTTAGAATTCGCCACCATGGCA 22AAGGGAGCCACC 16 3′ H60 GCGCTCGAGTCATTTTTTCTTC 23 AGCATACACCAAGRestriction sites inserted for cloning purposes are underlined.

Chimeric NKG2D was created by fusing the murine CD3ζ chain cytoplasmicregion coding sequence (CD3ζ-CYP) to the full-length gene of murineNKG2D. Briefly, the SalI-EcoRI fragment of CD3ζ-CYP (with the initiationcodon ATG at the 5′ end, primer numbers 9 and 10) and the EcoRI-XhoIfragment of NKG2D (without ATG, primer numbers 2 and 3) were ligatedinto the SalI/XhoI-digested pFB-neo retroviral vector (STRATAGENE®, LaJolla, Calif.). Similarly, chimeric Dap10 was generated by fusing theSalI-EcoRI fragment of full-length Dap10 (primer numbers 4 and 6) to theEcoRI-XhoI fragment of CD3ζ-CYP (primer numbers 11 and 12). Wild-typeNKG2D (primer numbers 2 and 3), Dap10 (primer numbers 4 and 5) and Dap12(primer numbers 7 and 8) fragments were inserted between the EcoRI andXhoI sites in pFB-neo. In some cases, a modified vector pFB-IRES-GFP wasused to allow co-expression of green fluorescent protein (GFP) withgenes of interest. pFB-IRES-GFP was constructed by replacing the 3.9 kbAvrUScaI fragment of pFB-neo with the 3.6 kb AvrII/ScaI fragment of aplasmid GFP-RV (Ouyang, et al. (1998) Immunity 9:745-755). Rae-1β(primer numbers 13 and 14) and H60 (primer numbers 15 and 16) cDNAs werecloned into pFB-neo. Constructs containing human NKD2D and human CD3ζ ormurine Fc were prepared in the same manner using the appropriate cDNAsas templates.

Example 3 Retrovirus Production and Transduction

Eighteen hours before transfection, Bosc23 cells were plated in 25 cm²flasks at a density of 4×10⁶ cells per flask in 6 mL of DMEM-10.Transfection of retroviral constructs into Bosc23 cells was performedusing LIPOFECTAMINE™ 2000 (INVITROGENT™, Carlsbad, Calif.) according tothe manufacturer's instruction. Viral supernatants were collected 48 and72 hours post-transfection and filtered (0.45 μm) before use. Forgeneration of large scale, high-titer ecotropic vectors, the ecotropicviruses produced above were used to transduce the dualtropic packagingcell PT67 in the presence of polybrene (8 μg/mL). After three rounds oftransduction, PT67 cells were selected in G418 (1 mg/mL) for 7 days.Dualtropic vectors were then used to transduce ecotropic cell lineGP+E86. Through this process, the virus titer from pooled GP+E86 cellsgenerally was over 1×10⁶ CFU/mL. Concentration of retroviruses bypolyethylene glycol (PEG) was performed according to standard methods(Zhang, et al. (2004) Cancer Gene Ther. 11:487-496; Zhang, et al. (2003)J. Hametother. Stem Cell Res. 12:123-130). Viral stocks with high titer(1˜2×10⁷ CFU/mL) were used for transduction of T cells. Primary T cellsfrom spleens of C57BL/6 (B6) mice were infected 18-24 hours afterconcanavalin A (ConA, 1 μg/mL) stimulation based on a well-establishedprotocol (Sentman, et al. (1994) J. Immunol. 153:5482-5490). Two daysafter infection, transduced primary T cells (0.5˜1×10⁵/mL) were selectedin RPMI-10 media containing G418 (0.5 mg/mL) plus 25 U/mL rHuIL-2 for anadditional 3 days. Viable cells were isolated using HISTOPAQUE®-1083(Sigma, St. Louise, Mo.) and expanded for 2 days without G418 beforefunctional analyses. NKG2D ligand-expressing RMA (RMA/Rae-1β andRMA/H60) or RMA-S (RMA-S/Rae-1β) cells were established by retroviraltransduction with dualtropic vectors from PT67.

Example 4 Cytokine Production by Gene-Modified T Cells

Gene-modified primary T cells (10⁵) were co-cultured with an equalnumber of RMA, RMA/Rae-1β, RMA/H60 or YAC-1 cells in 96-well plates incomplete media. After twenty-four hours, cell-free supernatants werecollected. IFN-γ was assayed by ELISA using a DUOSET® ELISA kits (R&D,Minneapolis, Minn.). In some cases, T cells were cultured with equalnumbers of irradiated (100 Gys) tumor cells for 3 days. Detection ofother cytokines in culture was performed using a BIO-PLEX® kit(BIO-RAD®, Hercules, Calif.) based on the manufacturer's protocol.

Example 5 Flow Cytometry

For FACS analysis of NKG2D ligand expression, tumor cells were stainedwith mouse NKG2D-Ig fusion protein (R&D systems) according tomanufacturer's instruction. Cell-surface phenotyping of transducedprimary T cells was determined by direct staining with APC-anti-CD3ε(clone 145-2C11; Pharmingen, San Diego, Calif.), PE-anti-NKG2D (clone16-10A1; eBioscience, San Diego, Calif.) and FITC-anti-CD4 (Clone RM4-5;Caltag, Burlingame, Calif.) monoclonal antibodies. Cell fluorescence wasmonitored using a FACSCALIBER™ cytometer. Sorting of NKG2Dligand-expressing cells was performed on a FACSTARM™ cell sorter (BectonDickinson, San Jose, Calif.).

Example 6 Cytotoxicity Assay

Three or four days after G418 selection (0.5 mg/mL), retroviralvector-transduced primary T cells were cultured in complete RPMI mediacontaining 25 U/mL human IL-2 for an additional 2-3 days. Viablelymphocytes were recovered by centrifugation over HISTOPAQUE®-1083(Sigma, St. Louis, Mo.) and used as effector cells. Lysis of targetcells (RMA, RMA/Rae-1β, RMA/H60, EG7, RMA-S, RMA-S/Rae-1β, and YAC-1)was determined by a 4-hour ⁵¹Cr release assay (Sentman, et al. (1994)supra). To block NKG2D receptors, anti-NKG2D (clone: CX5, 20 μg/mL) wasincluded in those assays. The percentage of specific lysis wascalculated as follows: % Specific lysis=[(Specific ⁵¹Crrelease−spontaneous ⁵¹Cr release)/(Maximal ⁵¹Cr release−spontaneous ⁵¹Crrelease)]×100.

Example 7 Treatment of Mice with Genetically Modified T Cells

For the determination of direct effects of chimeric NKG2D-bearing Tcells (10⁶) on the growth of RMA or RMA/Rae-1β tumors, chimeric NKG2D-or vector-transduced T cells were mixed with tumor cells (10⁵) and theninjected s.c. into the shaved right flank of recipient mice. Tumors werethen measured using a caliper, and tumor areas were calculated. Animalswere regarded as tumor-free when no tumor was found four weeks afterinoculation. For the rechallenge experiments, mice were inoculated with10⁴ RMA cells on the shaved left flank. In other experiments, transducedT cells were injected intravenously the day before s.c. inoculation oftumor cells. Mice were monitored for tumor size every two days and weresacrificed when tumor burden became excessive.

Example 8 Statistical Analysis

Differences between groups were analyzed using the student's t-test. pvalues<0.05 were considered significant.

1. A nucleic acid construct for expressing a chimeric polypeptidecomprising: a first nucleic acid sequence encoding a promoter operablylinked to a second nucleic acid sequence encoding a chimeric polypeptidecomprising DAP10 fused to a nucleic acid encoding an immune signalingreceptor containing an immunoreceptor tyrosine-based activation motif ofSEQ ID NO:1.
 2. The nucleic acid construct of claim 1, wherein theconstruct is in a vector.
 3. The nucleic acid construct of claim 1further comprising a suicide gene.
 4. (canceled)
 5. An isolated T cellcomprising the nucleic acid construct of claim 1 or 3, or the vector ofclaim 2.